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Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Hair loss in women may have causes other than hormones.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

Testosterone metabolism in balding scalp cells may not be the main cause of hair loss.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Assessing newborn scalp hair can reveal important health information.

Patient-derived melanocytes can potentially treat vitiligo by restoring skin pigmentation.

Artificial skin is improving wound healing and shows potential for treating different types of wounds.

Some skin medications can harm male fertility, but they don't seem to cause birth defects from father's exposure.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

A group has developed therapies that show promise for treating cancer and various other conditions.

A 10-year-old boy with abnormal genital development had surgery and tests to find the cause and plan treatment.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

Yellow dots look different in various hair loss conditions and can help diagnose them.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

FGF13 gene changes cause excessive hair growth in a rare condition.

Polonium poisoning is diagnosed by detecting it in urine and feces, and treated with supportive care, infection prevention, and chelation therapy.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.